BECKMAN COULTER ITA Control Serum Level 1 - Indonesia BPOM Medical Device Registration
BECKMAN COULTER ITA Control Serum Level 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220640. The device is manufactured by CLINIQA CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DHH TRADING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLINIQA CORPORATIONCountry of Origin
United States
Authorized Representative
PT. DHH TRADING INDONESIAAR Address
Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan
Registration Date
Apr 25, 2024
Expiry Date
Feb 10, 2026
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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